Dream of Accessible Transportation Comes True for New Jersey Family Living with Duchenne
Josvin and his family are relieved to have reliable transportation for medical appointments.
Welcome Packet
Been diagnosed or want to learn more?
Request a Packet
About Duchenne
Facts, Treatment, and Care
Read More
Duchenne News
The latest from our partners.
Read Now
Female Carriers
Resources, Care, and Programs
Community Ambassadors
Meet our Community Ambassadors
Clinical Trials
A quick look at investigational drug studies
Volunteer Opportunities
Ways to get involved and help raise funds and awareness for Duchenne.
Volunteer Today
Community Ambassadors
These ambassadors are Jett Foundation’s extra ears, eyes, and voice.
Toolkits
View our resources targeted toward volunteers.
Our Resources
Become a Partner
Learn about creating a partnership and joining our community.
Get Started
Host a Webinar
Learn about our community webinar series.
View Upcoming Webinars
Resource Library
Read about our resources for Partners.
Resources for Partners
How To Help
Make a difference in the lives of those living with Duchenne.
Get Started Volunteering
Clinical Trials
A quick look at investigational drug studies.
Read More About Clinical Trials
Duchenne News
Stay up to date with the latest discoveries.
Read Now
Book: Dan And DMD
This book will help parents and guardians as they prepare to talk to their children about Duchenne.
Read Here
Our Insurance Flight Plan
Our Health Insurance Flight Plan breaks down options that may be available to you.
Request a Flight Plan
Resource Library
Read about our resources for Medical Professionals.
Resources for Medical Professionals
About Female Carriers
Facts and information about female carriers.
Learn More
Resources for Carriers
Tools and materials for female carriers.
Read More
Connect with our Specialist
Get support and help navigating your journey.
Meet Trina
Carrier Conversations
Join a carrier support group session.
Upcoming Events
General Resources
Check out helpful tools and transition resources.
Find Resources
Transition Resources
GotTransition resources and tools.
Learn More
Camp Promise
Locations and information on how to apply.
Learn More
Community Webinars
Watch past recordings on care and resource topics.
Watch Now
Our Family Workshops bring together clinicians, researchers, and families impacted by Duchenne in many cities each year. Community Webinars better prepare our community through virtual speakers and presentations.
Jett Foundation knows and understands that getting a diagnosis like Duchenne is far from easy. We have worked to create a package for families on this journey –through its highs and lows.
Our Community Webinar Series is focused on ensuring that our Duchenne community is better prepared for those unexpected moments, challenging medical decisions, and difficult stages when on a Duchenne journey.
This program aims to spread awareness about Duchenne and the programs and services that Jett Foundation provides through community ambassadors, who are individuals with Duchenne, parents, family, and more.
Josvin and his family are relieved to have reliable transportation for medical appointments.
Victor, Christian, and Alan Cruz look forward to unencumbered travel to medical appointments and daily activities.
The Petz family’s van opens opportunities for family trips, safe everyday travels, and countless memories.
Ethan Hoot has more freedom and independence to explore his childhood with accessible transportation.
Massachusetts residents Natalie, Paul and their 29-year-old son Max Gaudenzi have been navigating a life with Duchenne muscular dystrophy since Max was diagnosed at a
Fourteen-year-old Cooper Klein from Pasadena, Maryland, lives with Duchenne muscular dystrophy, a progressive neuromuscular disorder that weakens his muscles and affects his lungs and heart.
The Partin-Rockwood Family has three boys living with Duchenne and autism who are excited for new adventures.
Ellis Bautista and his family celebrate the arrival of safe and accessible transportation.
Daniel Toy and his family look forward to many adventures and memories thanks to new accessible van.
The Fialkowski Family celebrates the ability to safely transport their family again.
The Kim Family starts a new journey of safe and accessible transportation.
Arian Mooring is an 13-year-old boy living in Goldsboro, North Carolina, with his grandparents and younger brother, Slayden. Diagnosed at 15 months old, Arian is
Jett Foundation, Inc.
65 Cordage Park Circle
Suite 130 | Plymouth, MA 02360
781-585-5566 | [email protected]
Sign up to receive our newsletter and updates.
Required fields are denoted with an asterisk (*)
Tune in on February 29 to hear from our panel and moderators on how they are accomplishing goals and living life to the fullest!
Your gift helps Jett Foundation provide programming and opportunities, such as Camp Promise, to many families impacted by Duchenne muscular dystrophy each year.